Term ID: |
31416 |
Name: |
Abnormal nasal mucus secretion |
Synonym: |
|
Definition: |
Any deviation from the normal quantity of secretion of nasal mucus, a thick viscous liquid produced by the mucous membranes of the nose. |
Comments: |
|
Reference: |
HP:0031416 |
Genes and Diseases: | |
Child Nodes: |
........Rhinorrhea (HP:0031417) |
Sister Nodes: |
..Abnormal blood gas level (HP:0012415)
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..Abnormal breath sound (HP:0030829)
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..Abnormal bronchus physiology (HP:0025427)
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..Abnormal mucociliary clearance (HP:0031602)
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..Abnormal pattern of respiration (HP:0002793)
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..Abnormal respiratory motile cilium physiology (HP:0012261)
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..Abnormal response to short acting pulmonary vasodilator (HP:0030893)
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..Abnormality of pulmonary circulation (HP:0030875)
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..Abnormality on pulmonary function testing (HP:0030878)
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..Airway obstruction (HP:0006536)
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..Aspiration (HP:0002835)
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..Asthma (HP:0002099)
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..Breathing dysregulation (HP:0005957)
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..Cough (HP:0012735)
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..Cyanosis (HP:0000961)
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..Dyspnea (HP:0002094)
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..obsolete Decreased pulmonary function (HP:0005952)
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..Recurrent singultus (HP:0100247)
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..Reduced vital capacity (HP:0002792)
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..Respiratory insufficiency (HP:0002093)
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..Restrictive ventilatory defect (HP:0002091)
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..Sneeze (HP:0025095)
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..Snoring (HP:0025267)
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..Tracheal tug on inspiration (HP:0025008)
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..Upper airway obstruction (HP:0002781)
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..Weakness of muscles of respiration (HP:0004347)
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Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: | HPO disease - gene - phenotype less frequent non-typical associations: | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | CCDC39 CL E G H | 339829 | 25244 | OMIM:613807 | Ciliary dyskinesia, primary, 14 | | | | 126 | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | CCDC40 CL E G H | 55036 | 26090 | OMIM:613808 | CILIARY DYSKINESIA, PRIMARY, 15; CILD15 | | | | 182 | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | DNAH1 CL E G H | 25981 | 2940 | OMIM:617577 | Ciliary dyskinesia, primary, 37 | | | | 21 | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | LRRC56 CL E G H | 115399 | 25430 | OMIM:618254 | CILIARY DYSKINESIA, PRIMARY, 39; CILD39 | | | | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | ODAD1 CL E G H | 93233 | 26560 | OMIM:615067 | Ciliary dyskinesia, primary, 20 | | | | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | SCN9A CL E G H | 6335 | 10597 | OMIM:167400 | Paroxysmal extreme pain disorder | | | | 318 | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:100093 | Carcinoid syndrome | | | | 129 | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | SREBF1 CL E G H | 6720 | 11289 | OMIM:158310 | Mucoepithelial dysplasia, hereditary | | | | 1 | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | CCDC39 CL E G H | 339829 | 25244 | OMIM:613807 | Ciliary dyskinesia, primary, 14 | | | | 126 | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | CCDC40 CL E G H | 55036 | 26090 | OMIM:613808 | CILIARY DYSKINESIA, PRIMARY, 15; CILD15 | | | | 182 | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | DNAH1 CL E G H | 25981 | 2940 | OMIM:617577 | Ciliary dyskinesia, primary, 37 | . | | | 21 | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | LRRC56 CL E G H | 115399 | 25430 | OMIM:618254 | CILIARY DYSKINESIA, PRIMARY, 39; CILD39 | | | | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | ODAD1 CL E G H | 93233 | 26560 | OMIM:615067 | Ciliary dyskinesia, primary, 20 | . | | | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | SCN9A CL E G H | 6335 | 10597 | OMIM:167400 | Paroxysmal extreme pain disorder | . | | | 318 | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | SDHD CL E G H | 6392 | 10683 | ORPHA:100093 | Carcinoid syndrome | HP:0040283 - Occasional | | | 129 | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | SREBF1 CL E G H | 6720 | 11289 | OMIM:158310 | Mucoepithelial dysplasia, hereditary | . | | | 1 | | |
Genes (8) :CCDC39 CCDC40 DNAH1 LRRC56 ODAD1 SCN9A SDHD SREBF1
Diseases (8) :OMIM:613807 OMIM:613808 OMIM:617577 OMIM:618254 OMIM:615067 OMIM:167400 ORPHA:100093 OMIM:158310 |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
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